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JOBS! | Send Us Your Resume | Email Me
Companies:  Let Us Know Your Key Personnel Needs

James Walkup, Executive Recruiter

Jim Walkup, Vice President, Executive Recruiter, BSBA from University of Alabama. Jim serves the Pharmaceutical, Medical Device, Biotech and Health and Beauty Aids Industries.

Jim recruits professional candidates, management, R&D Technical, QC/QA, manufacturing, engineering and other professionals for the above industries.

JOBS

Your resume is held in strict confidence, all fees are employer paid, and relocation assistance is provided for all qualified persons unless otherwise stated.

Updated February 2008

Research & Development-Senior Scientist (Formulations) - BS Chemistry or related; 4 years experience.  5-8 years experience in formulations, with exposure to process development, scale-up, pilot plant and technology transfer from bench to manufacturing plant.  Responsible for developing new personal care product formulas and reformulating/improving current formulas; technical instruction and guidance; develop robust manufacturing processes; develop specifications for insuring NBE quality; and source/approve new
and/or alternate raw materials.  $50-66K.  Tennessee (SP)
QC Supervisor (ICP) Inductively Coupled Plasma - 4-year science degree.  Responsible for all group functions including: scheduling, testing, calibrations, instrument maintenance, inventory control, training, methods development, validations and participated hiring.  Conduct research, quantitative and qualitative analysis and experimentation on substances for such purposes as raw material/finished product release and stability testing vs compendial and in-house specifications.  $55-65K.  Pennsylvania.  (SP)
Research Scientists (3) - Company is leader in development, manufacture and sales of first-class generic pharmaceuticals with operations in 32 countries, products registered in more than 60 countries, a robust development pipeline and an aggressive acquisition strategy.  All located in New Jersey.
  1. Research Scientist - Evaluate raw material samples from alternate source candidates, using existing or modified methods to determine compliance.  HPLC, Laser Diffraction, Gas Chromatography, Documentation.  BS Chemistry or related.  Minimum 5 years Pharma analytical testing.  $70-80K (SP)
  2. Associate Research Scientist or Research Scientist - Conduct routine testing/method validation for residual solvent by GC methods; support formulators for development sample testing.  BS Chemistry.  5+ years experience in generic Pharma industry in QC or AD.  cGMP.  $70K+  (SP)
  3. Associate Research Scientist - Develop/validate analytical methods for ANDA candidate formulations.  Routing testing as required.  Prepare documents including protocols, methods, reports for method validation and related.  cGMP, HPLC.  BS Chemistry.  2-3 years experience in generic Pharma industry.  $60-70K (SP)
Formulation Scientist - MS/PhD. 5+ years Pharmaexperience. 5 years experience in formulation and testing. Experience in formulating/testing with solid dosage products.  Design, formulate, process, optimize, test Pharma dosage forms to determine effect of formulation and processing variables on product and impact on bioavailability and bioequivalence.  $70-l00K. North Carolina. (SP)
Manager Plant Operations-Pharmaceuticals - Classic change agent for operations role for large 800 employee location for Medical manufacturer.  Responsible for manufacturing operations.  Black Belt/Lean Certified a plus.  Engineering or Life Science degree preferred.  Six Sigma.  API products.  $145-160K.  Missouri (BL)
Director of Quality - 10+ years experience.  Heads quality/Technical
Department-supervisory.  Quality Functions: reviews trends, prepares/writes annual product reviews, oversees validation program, oversees calibration program, development, writing, editing, review and approving SOPs, auditing, review labeling, customer complains, technical services.  $85-95K = 5-10% bonus.  Georgia (SP)
Lab Manager & Assistant Lab Manager - Manager = 5+ years experience, $80-90K  Assistant Manager = 1-2 years experience, $60-70K.  Pharm or hair and beauty aids experience.  BS Chemistry.  Technical background.  IQ, OQ, PQ and Part
1; cGMP/GLP.  Proficient in development/implementing controls/documentation.  Massachusetts. (SP)
Applications Development Group Manager - MS Food Service/Engineering or related.  5 years technical R&D experience; 3 years management experience.  Responsible for actively assuring RAI new product growth objectives through direct management of the group responsible for the identification, development, implementation of technical projects/programs across all commercial applications for Food/Industrial markets.  $79-88K - 18% bonus
target group.  Iowa. (SP)
Regional Sales Associate Program Coordinator - Required:  BS (pharmacology, chemistry, biology).  1-3 industry experience in tech and sales field.  Travel = 50%.  Responsible for planning, managing, coordinating execution of Pharmaceutical, Nutraceutical, Oral Care strategy across a variety of market areas within an assigned geographic territory for purpose of generating significant new sales, value and achieving the agreed objects.  $75-85K.  California. (SP)
Senior Research Scientist-Medicinal Chemistry - PhD organic
chemistry/medicinal chemistry.  3-5 years Pharma process research
experience.  Adept in multiple scientific disciplines including process
chemistry, organic chemistry and medicinal chemistry.  GLP, GMP.   Develop methods/procedures for scale-up of proprietary compounds selected for preclinical development.  Work in collaboration with external manufacturing organizations to successfully scale-up the synthesis of sufficient quantities of lead molecules for preclinical and clinical development.  Create technical process transfer documents.  Determine purity of products.  Collaborate with medicinal chemists to accelerate lead compound synthesis for screening and development.  $100K+.  Tennessee (GB)
QC Chemist - Analytical Chemist.  Method development and validation experience for HPLC and GC assays, along with experience in performing the typical QC testing for raw materials, in-process, intermediates, release and stability in GMP lab.  Experience with GMP documentation practices a must.  $55K base, bonus potential.  Western, NC (LD)
Quality Systems Manager - BS degree in engineering/scientific.  8 yeas Pharma QA experience.  Six Sigma.  Manage quality systems/compliance efforts to include documentation, complaint handling, tech transfers, product release, validation, FDA interaction, audits, allied areas.  Prefer local candidate.  $100K.  New Jersey (JC)
Formulation Scientist - BS engineering/scientific.  4 years experience in formulation of nutritional products.  Knowledge of development of products with multiple ingredients, vitamins, minerals, uniformity and stability issues.  Report to Director of R&D.  Responsible for solid dosage form formulation of Pharma and nutritional products for a leading OTC products company.  $75-75K.  Utah.  (JC)
Manager/Sr. Manager Business Development - Call on other Pharma companies and develop CMO relationships for client.  Great company and super quality of life.  No more than 10-15% travel.  $10K + bonus.  North Carolina  (LD)
Technical Operations Manager-formulations - BS/MS Chemistry/Engineering.  Experience in formulations, Microsoft Office.  Strong analytical and communication skills.  5 years experience in Technical Operations/product Development.  Direct and oversee policies, objectives, schedules, initiatives of Tech Operations.  Maintain companies' competitive position and profitability.  Supervisory and direct lab work.  CGMP.  Nutritional
products company.  North Carolina.  (LD)
ADDITIONAL POSITIONS SP ASSOCIATES, INC. IS RECRUITING FOR:
 
Three positions in Eastern NJ - Good company, very nice location.  Base to $110K or so, bonus.  Nice moving package.  QA manager, QC Labs Manager (Chemistry & Micro), Validation Manager. Pharma background required. Experience with SVPs would be nice, but not essential. (LD)
 
Six positions located in RTP, NC - All positions need parenterals
experience.  Engineering Manager/Director - facilities, utilities, etc.  To $115K.  Validation Manager - $80-90K.  Microbiology Manager - $80-90K.  2-Process Engineers - $75K.  Project Manager - Mid $80's. (LD)

Four positions located in Ridgefield Park, NJ - Associate Director,

Postmarketing Regulatory Affairs - $210K + bonus.  Associate Director (CNS) Regulatory Affairs - to $210K + bonus.  Associate Director, Regulatory Affairs, Oncology - to $210K + bonus.  Associate Director, Regulatory Affairs, Sepsis/GI - to $210K + bonus. (RS)

QC Analysts (2):

Perform analyses on samples which may include in-process material, finished products, raw materials, production stability samples and process validations using chemical, physical, and instrumental analytical procedures. Analyze samples according to current methods to ensure the highest quality product that meets specification. Monitor and verify quality at every step in the testing process.  The successful candidate will have knowledge of controlled release rotating bottle baths, USP dissolution equipment, Technicon auto analyzers, Gas chromatography (GC), high pressure liquid chromatography (HPLC), atomic absorption (AA), infrared spectrophotometer (IR), ultraviolet/visible spectrophotometer (UV/VIS), pH meter, flurometer, melting point apparatus, viscometers, muffle furnace, polarimeter, vacuum oven, distillations, titrations, centrifuge, sonicator, conductivity meter. Familiarity with compendial guidelines such as USP, EP as well as a LIMS system and knowledge of regulatory guidelines such as cGMP are also required.  Location:  Missouri   Salary:  $60K+

2 – QC Analysts – 2nd shift – Solid dosage, dissolution is a plus – HPLC 

QC Supervisors (4):

Primary responsibilities include supervision of the daily operation of assigned shift including oversight for testing, reviewing test results, and distributing release information. The successful candidate will oversee the laboratory for cGMP/GLP and safety compliance. You will have the opportunity to participate in the introduction of new methodology and equipment into the Analytical laboratory. We are seeking qualified individuals with experience interfacing with other departments regarding QC testing, training on QC procedures, initiating and directing OOS investigations, and generating status and backlog reports and writing and updating compendia and non-compendia methods for use by the analysts. Previous supervisory experience is a must.  Location:  Missouri   Salary: $90K

1 – QC Supervisor – 1st shift (M-F) – Raw Materials – Wet Chemistry, little HPLC

1 – QC Supervisor – 2nd shift (Tu – Sat) – Solid dosage, dissolution is a plus – HPLC

1 – QC Supervisor – 2nd shift (Sun – thurs) – Solid dosage, dissolution is a plus – HPLC

1 – QC Supervisor – 3rd Shift (Sun – Thur) – Solid dosage, dissolution is a plus – HPLC

Updated February 2008

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Toll Free:  (866)488-6677 | Phone:  (704)643-7250 | Fax:  (704)643-1249 | Email:  jwalkup@spassociates.com

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